Method for determining antagonist activity to a cytokinin receptor

ABSTRACT

The present invention provides a method for analyzing agonist-activity to a cytokinin receptor, which comprises (1) bringing an examinee substance into contact with a transformed cell into which DNA coding the cytokinin receptor is introduced and (2) measuring the existence or the quantity of intracellular signal transduction from the cytokinin receptor expressed in the transformed cell, and, a method for analyzing antagonist-activity to a cytokinin receptor, which comprises (1) bringing an examinee substance and a substance having agonist-activity to the cytokinin receptor into contact with a transformed cell into which DNA coding the cytokinin receptor is introduced.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a divisional of allowed U.S. application Ser. No.12/773,456 filed May 4, 2010, which is a divisional of application Ser.No. 09/918,508 filed Aug. 1, 2001 (now U.S. Pat. No. 7,741,049), whichclaims priority to JP 2001-073812, filed Mar. 15, 2001. The entiredisclosures of the prior applications are incorporated herein byreference in their entirety.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to a method for analyzing agonist-activityand antagonist-activity of an examinee to cytokinin receptor.

2. Description of the Related Art

Cytokinins are plant hormones relevant to cell division anddifferentiation of higher plants and are well-known as very importantphysiologically active substances having functions of inducing divisionof cells of higher plants, differentiating the callus and pith to thestems and leaves, ethiolating and defoliating leaves, preventing thefalling of fruit, breaking the dominance of the terminal bud and thelike [Cytokinins: Chemistry, Activity, and Function, CRC Press (1994)].The substances having cytokinins-like activities are usable as plantgrowth regulators, for example, fruit-falling preventive agents forfruits such as apple, orange, and the like, plant-falling preventiveagents for rice plants, barley, wheat and the like by regulating theheight of the plants, and sweetness increasing agents for fruits afterharvest.

As a method for finding substances having such cytokinins-likeactivities, conventionally employed is a method for observing andevaluating the physiological changes by directly spraying examineesubstances to plant.

The aforementioned method has problems that it requires to prepare theexaminee substances in amounts sufficient to directly spray them toplant and also requires immensely long time to observe and evaluate thegrowth of the plant and the physiological changes of the plant afterspraying of the examinee substances. Therefore, it has been required fora long to develop a variety of methods for quickly finding substanceshaving cytokinins-like activities with small amounts of examineesubstances.

SUMMARY OF THE INVENTION

Inventors of the present invention have intensively investigated in suchsituations and first found protein functioning as a cytokinin receptorand subsequently found it possible to analyze the agonist-activity andthe antagonist-activity of examinee substances to a cytokinin receptorby using the cytokinin receptor (“the analysis method”) and also it ispossible to quickly search substances having cytokinins-like activitieseven in a small amount of examinee substances by employing the analysismethod and consequently reached the present invention.

The present invention provides:

1: A method for analyzing agonist-activity to a cytokinin receptor,which comprises (1) bringing an examinee substance into contact with atransformed cell into which DNA coding the cytokinin receptor isintroduced and (2) measuring the existence or the quantity ofintracellular signal transduction from the cytokinin receptor expressedin the transformed cell.

2: The method according to the above 1, wherein the transformed cell isa cell having a function of directly controlling the cell growth byintracellular signal transduction from the cytokinin receptor and themeasurement of the existence or the quantity of the intracellular signaltransduction is carried out using the quantity of the cell growth of thetransformed cell as an indicator.

3: The method according to the above 1, wherein the transformed cell isa transformed cell generated by introducing DNA coding the cytokininreceptor into a host cell so improved as to have histidine kinaseactivity lower than the intrinsic histidine kinase activity of the hostcell.

4: The method according to the above 1, wherein the transformed cell isa transformed cell generated by introducing DNA coding the cytokininreceptor into a host cell so improved as to have histidine kinaseactivity lower than the intrinsic histidine kinase activity of the hostcell by deleting one or more of histidine kinase.

5: The method according to the above 1, wherein the transformed cell isa transformed cell generated by introducing DNA coding the cytokininreceptor into a host cell having no cytokinin receptor.

6: The method according to the above 1, wherein the transformed cell isyeast.

7: The method according to the above 1, wherein the transformed cell isbudding yeast.

8: The method according to the above 1, wherein the DNA coding thecytokinin receptor is any one of DNA coding the cytokinin receptorselected from:

(a) a cytokinin receptor having the amino acid sequence represented bySEQ ID No: 6;

(b) a cytokinin receptor having the amino acid sequence represented bySEQ ID No: 2;

(c) a cytokinin receptor having the amino acid sequence represented bySEQ ID No: 4;

(d) a cytokinin receptor wherein said cytokinin receptor has at leastone transmembrane region but less than that in its natural form;

(e) a cytokinin receptor having the amino acid sequence from amino acidnumber 196 to 1176 among the amino acid sequence represented by SEQ IDNo: 2;

(f) a cytokinin receptor having the amino acid sequence from amino acidnumber 50 to 1176 among the amino acid sequence represented by SEQ IDNo: 2;

(g) a cytokinin receptor having the amino acid sequence from amino acidnumber 32 to 1036 among the amino acid sequence represented by SEQ IDNo: 4;

(h) a chimera-type cytokinin receptor comprising extracellular regionsof the cytokinin receptor, transmembrane regions of the cytokininreceptor, and histidine kinase regions of the cytokinin receptor,wherein each of the regions is a homogeneous region to one another andreceiver regions for the histidine kinase, which are heterogeneousregions to these regions; and

(i) a cytokinin receptor having the amino acid sequence with deletion,substitution, or addition of one or a plurality of amino acids in theamino acid sequence of the cyctokinin receptor of (a), (b), (c), (e),(f), or (g).

9: A method for analyzing antagonist-activity to a cytokinin receptor,which comprises (1) bringing an examinee substance and a substancehaving agonist-activity to the cytokinin receptor into contact with atransformed cell into which DNA coding the cytokinin receptor isintroduced and

(2) measuring the existence or the quantity of intracellular signaltransduction from the cytokinin receptor expressed in the transformedcell.

10: The method according to the above 9, wherein the transformed cell isa cell having a function of directly controlling the cell growth byintracellular signal transduction from the cytokinin receptor and themeasurement of the existence or the quantity of the intracellular signaltransduction is carried out using the quantity of the cell growth of thetransformed cell as an indicator.

11: The method according to the above 9, wherein the transformed cell isa transformed cell generated by introducing DNA coding the cytokininreceptor into a host cell so improved as to have histidine kinaseactivity lower than the intrinsic histidine kinase activity of the hostcell.

12: The method according to the above 9, wherein the transformed cell isa transformed cell generated by introducing DNA coding the cytokininreceptor into a host cell so improved as to have histidine kinaseactivity lower than the intrinsic histidine kinase activity of the hostcell by deleting one or more of histidine kinase.

13: The method according to the above 9, wherein the transformed cell isa transformed cell generated by introducing DNA coding the Cytokininreceptor into a host cell having no cytokinin receptor.

14: The method according to the above 9, wherein the transformed cell isyeast.

15: The method according to the above 9, wherein the transformed cell isbudding yeast.

16: The method according to the above 9, wherein the DNA coding thecytokinin receptor is any one of DNA coding the cytokinin receptorselected from:

(a) a cytokinin receptor having the amino acid sequence represented bySEQ ID No: 6;

(b) a cytokinin receptor having the amino acid sequence represented bySEQ ID No: 2;

(c) a cytokinin receptor having the amino acid sequence represented bySEQ ID No: 4;

(d) a cytokinin receptor wherein said cytokinin receptor has at leastone transmembrane region but less than that in its natural form;

(e) a cytokinin receptor having the amino acid sequence from amino acidnumber 196 to 1176 among the amino acid sequence represented by SEQ IDNo: 2;

(f) a cytokinin receptor having the amino acid sequence from amino acidnumber 50 to 1176 among the amino acid sequence represented by SEQ IDNo: 2;

(g) a cytokinin receptor having the amino acid sequence from amino acidnumber 32 to 1036 among the amino acid sequence represented by SEQ IDNo: 4;

(h) a chimera-type cytokinin receptor comprising extracellular regionsof the cytokinin receptor, transmembrane regions of the cytokininreceptor, and histidine kinase regions of the cytokinin receptor,wherein each of the regions is a homogeneous region to one another andreceiver regions for the histidine kinase, which are heterogeneousregions to these regions; and

(i) a cytokinin receptor having the amino acid sequence with deletion,substitution, or addition of one or a plurality of amino acids in theamino acid sequence of the cyctokinin receptor of (a), (b), (c), (e),(f), or (g).

17: A cytokinin receptor selected from:

(d) a cytokinin receptor wherein said cytokinin receptor has at leastone transmembrane region but less than that in its natural form;

(e) a cytokinin receptor having the amino acid sequence from amino acidnumber 196 to 1176 among the amino acid sequence represented by SEQ IDNo: 2;

(f) a cytokinin receptor having the amino acid sequence from amino acidnumber 50 to 1176 among the amino acid sequence represented by SEQ IDNo: 2;

(g) a cytokinin receptor having the amino acid sequence from amino acidnumber 32 to 1036 among the amino acid sequence represented by SEQ IDNo: 4;

(h) a chimera-type cytokinin receptor comprising extracellular regionsof the cytokinin receptor, transmembrane regions of the cytokininreceptor, and histidine kinase regions of the cytokinin receptor,wherein each of the regions is a homogeneous region to one another andreceiver regions for the histidine kinase, which are heterogeneousregions to these regions; and

(i) a cytokinin receptor having the amino acid sequence with deletion,substitution, or addition of one or a plurality of amino acids in theamino acid sequence of the cyctokinin receptor of (e), (f), or (g).

18: DNA coding the cytokinin receptor of the above 17.

19: A transformed cell into which DNA of the above 18 is introduced.

20: A method for detecting agonist-activity to a cytokinin receptor,which comprises evaluating the agonist-activity of two or more differentexaminee substances to the cytokinin receptor based on the differenceobtained by comparison of the existence or the quantity of theintracellular signal transduction in a section where the examineesubstances are independently used and measured by the analysis method ofthe above 1.

21: The method according to the above 20, wherein at least one substanceamong the two or more different examinee substances is a substancehaving no agonist-activity to the cytokinin receptor.

22: A method for searching agonist-active substance to a cytokininreceptor, which comprises selecting a substance having agonist-activityto a cytokinin receptor based on the agonist-activity to a cytokininreceptor evaluated by the detecting method of the above 20.

23: A plant growth regulator comprising the substances selected by thesearching method of the above 22 as an active ingredient.

24: A method for detecting antagonist-activity to a cytokinin receptor,which comprises evaluating the antagonist-activity of two or moredifferent examinee substances to the cytokinin receptor based on thedifference obtained by comparison of the existence or the quantity ofthe intracellular signal transduction in a section where the examineesubstances are independently used and measured by the analysis method ofthe above 9.

25: The method according to the above 24, wherein at least one substanceamong the two or more different examinee substances is a substancehaving no antagonist-activity to the cytokinin receptor.

26: A method for searching antagonist-active substance to a cytokininreceptor, which comprises selecting a substance havingantagonist-activity to a cytokinin receptor based on theantagonist-activity to a cytokinin receptor evaluated by the detectingmethod of the above 24.

27: A plant growth regulator comprising the substances selected by thesearching method of the above 26 as an active ingredient.

Further scope of applicability of the present invention will becomeapparent from the detailed description given hereinafter. However, itshould be understood that the detailed description and specificexamples, while indicating preferred embodiments of the invention, aregiven by way of illustration only, since various changes andmodifications within the spirit and scope of the invention will becomeapparent to those skilled in the art from this detailed description.

Throughout this specification and the claims which follow, unless thecontext requires otherwise, the word “comprise”, and variations such as“comprises” and “comprising”, will be understood to imply the inclusionof a stated integer or step or group of integers or steps but not theexclusion of any other integer or step or group of integers or steps.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

Hereinafter, the present invention will be described in detail.

A cytokinin receptor is protein having functions of controlling thepropagation and differentiation of cells of higher plants based on theintracellular signal transduction mechanism so-called Two-Componentregulatory system (or Histidine to Aspartic acidartic acid phosphorelaysystem) while being specifically bonded with cytokinins such as purinetype cytokinins, e.g. kinetin, zeatin, and the like, and urea typecytokinins, e.g. N-phenyl-N′-(4-pyridyl)urea and the like. The cytokininreceptor to be used in the present invention belongs to the histidinekinase family and is protein composed of extracellular regions,transmembrane regions, histidine kinase regions (regions havinghistidine kinase activity in the cell and holding Histidine residue tobe an active site), and receiver regions (regions having a receptionpart for phosphate group transfer and holding Aspartic acid residue tobe an active site).

Practical examples of the cytokinin receptor are cytokinin receptorshaving the amino acid sequences represented by SEQ ID Nos: 2, 4, and 6,cytokinin receptors having the amino acid sequences represented by SEQID Nos: 2, 4, and 6 wherein one or a plurality of amino acids aredeleted, substituted, or added, cytokinin receptors having the aminoacid sequences coded with DNA to be hybridized in stringent conditionswith DNA having the nucleotide sequences coding the amino acid sequencesrepresented by SEQ ID Nos: 2, 4, and 6, cytokinin receptors of partiallytransmembrane region-deleted type which will be described later, andchimera-type cytokinin receptors which will be described later, and thelike. Incidentally, the phrase, “a plurality of amino acids”, means moreparticularly about 2 to 20 amino acids and for example, 2 to 10 aminoacids and 2 to 5 amino acids may be exemplified. Also, the phrase, “theamino acid sequences . . . wherein one or a plurality of amino acids aredeleted, substituted, or added”, means as examples those having theamino acid sequences of which 80% or higher, preferably 90% or higher,and more preferably 95% or higher are identical with the sequences ofthe amino acids before the deletion, substitution or addition of aminoacids (i.e. amino acid sequence identification of 80% or higher,particularly 90% or higher, and more preferably 95% or higher).

Those phrases, “deletion, substitution or addition of amino acids” or“which 80% or higher . . . are identical” of course include theintracellular processing to which proteins having the amino acidsequences represented by SEQ ID Nos: 2, 4, and 6 are subjected, and thenatural variations caused by differences in type of organisms from whichthe proteins are derived, differences in individual bodies, differencesin tissues, and the like.

The phrase, “sequence identification”, in the present invention meansthe identification and homology between two DNA sequences and betweentwo protein sequences. The sequence identification may be determined bycomparing two sequences aligned in the optimum states in a region of thesequences of the comparison objects. The DNA or proteins, the comparisonobjects, may have addition or deletion (e.g. gap and the like) in theoptimum alignment of two sequences. Regarding such sequenceidentification, computation may be performed using, for example, VectorNTI by producing alignment by utilizing Clusta 1W algorithm [NucleicAcid Res., 22 (22): 4673-4680 (1994)]. Incidentally, the sequenceidentification may be measured by a sequence analysis soft, practicallyVector NTI, GENETYX-MAC and analysis tools provided in public database.

Regarding the phrase, “be hybridized in stringent conditions”, the term,hybridization, in this case may be performed, for example, according toa common method described in Molecular Cloning 2nd edition, written bySambrook J., Frisch E. F., Maniatis T., issued by Cold Spring HarborLaboratory Press. Further, the phrase, “in stringent conditions”, means,for example, that a hybrid is formed in a solution of 6×SSC (a solutioncontaining 1.5 M NaCl and 0.15 M trisodium citrate is defined as 10×SSC)at 65° C. and then washed with 1×SSC at a room temperature. The saltconcentration in the washing step may be selected, for example, from thecondition of 1×SSC at a room temperature (a low stringent condition) to0.1×SSC at a room temperature (a high stringent condition). Thetemperature in the washing step may be selected, for example, from aroom temperature (a low stringent condition) to 68° C. (a high stringentcondition). Further, both of the salt concentration and the temperaturemay be changed.

(Production of a Transformed Cell into Which DNA Coding a CytokininReceptor is Introduced)

A transformed cell into which DNA coding a cytokinin receptor isintroduced may be obtained by introducing and expressing DNA coding thecytokinin receptor, that is, DNA having nucleotide sequence coding theamino acid sequence of the cytokinin receptor in a host cell in thefollowing manner. Hereinafter, one example of the method of theproduction of a transformed cell will be described.

(1) Preparation of cDNA

At first, the total RNA is prepared from plants such as higher plantsaccording to the method described in Molecular Cloning 2nd editionwritten by J., Sambrook, E., F., Frishch, T., Maniastis.

Concretely, for example, after a part of tissues are sampled from ahigher plant such as a monocotyledonous plant, e.g. rice, corn, barley,wheat and the like and a dicotyledonous plant, e.g. tobacco, soybean,Arabidopsis, and the like and then the tissues are frozen in liquefiednitrogen and successively physically milled using a mortar and pestle orthe like and after that, either (a) the resulting milled product ismixed with a solution containing guanidine hydrochloride with phenol orSDS with phenol to obtain the total RNA or (b) the resulting milledproduct is mixed with a solution containing guanidine thiocyanate andfurther with CsCl and then subjected to centrifugal separation to obtainthe total RNA. For the aforementioned process, commercialized kits suchas ISOGEN (produced by Nippon Gene Co.), RNeasy Total RNA PurificationKit (produced by QIAGEN Co.), and the like may be employed.

Next, mRNA is prepared from the total RNA. For example, the preparationmay be carried out by a method utilizing the hybridization of oligo-dTchains bonded with cellulose or latex and poly-A chains of mRNA. For theoperation, for example, commercialized kits such as mRNA PurificationKit (produced by Amersham Pharmacia Co.), OLIGOTEX™ dt30 super (Oligo(dT) latex beads) (produced by Takara Shuzo Co. Ltd.), and the like maybe employed.

Further, cDNA is produced using the mRNA (mRNA having poly-A chains)prepared in such a manner. For example, oligo-dT chains or randomprimers are annealed with mRNA and then reacted with reversetranscriptase to produce cDNA. Further, the cDNA is reacted with, forexample, RNaseH, DNA polymerase Ito produce double chain cDNA. For theoperation, for example, the following commercialized kits may beemployed: SMART™ PCR cDNA Synthesis Kit (produced by Clontech Co.), cDNASynthesis Kit (produced by Takara Shuzo Co. Ltd.), cDNA Synthesis Kit(produced by Amersham Pharmacia Co.), ZAP-cDNA Synthesis Kit (producedby Stratagene Co.) and the like.

(2) Cloning

The DNA coding the cytokinin receptor may be obtained by a polymerasechain reaction (hereinafter referred as to PCR) from the produced cDNAusing, for example, DNA having partial nucleotide sequence of thenucleotide sequence of SEQ ID No: 1, 3 or 5 as a primer or by ahybridization method using DNA having partial nucleotide sequence of thenucleotide sequence of SEQ ID No: 1, 3 or 5 as a probe.

In the case of employing PCR, DNA usable as a primer set is thoseplanned and synthesized based on the nucleotide sequences of about 20 byto 40 bp, for example, the nucleotide sequences selected respectivelyfrom 5′-non-translation regions and 3′-non-translation regions of thenucleotide sequence represented by SEQ ID No: 1, 3, or 5. Examples ofthe primer set are sets of DNA of nucleotide sequence represented by SEQID No: 9 and DNA of nucleotide sequence represented by SEQ ID No: 10.The PCR solution to be used may be prepared by adding reaction solutionsinstructed by the kit to cDNA 250 ng. The conditions of the PCR mayproperly be changed depending on the primer set to be used and, forexample, concrete conditions include as follows: keeping at 94° C. for 2minutes, at about 8° C. for 3 minutes, and further repeating 40 cycleseach of which comprises steps of keeping at 94° C. for 30 seconds, at55° C. for 30 seconds, and at 72° C. for 4 minutes; and repeating 5 to10 cycles each of which comprises steps of keeping at 94° C. for 5seconds and at 72° C. for 4 minutes and further repeating about 20 to 40cycles each of which comprises steps of keeping at 94° C. for 5 secondsand at 70° C. for 4 minutes. For the operation, the followingcommercialized kits may be, for example, employed: HERCULASE™ (producedby Stratagene), DNA polymerase contained in Advantage cDNA PCR Kit(Clontech Co.), TAKARA Ex Taq (Takara Shuzo Co., Ltd.), PLATINUM™ PCRSUPER (thermostable DNA polymerase in a PCR reaction mix) (LifetechOriental Co.), and the like.

In the case of employing hybridization, cloning may be carried outaccording to a method described in, for example, “Cloning and Sequence”,Experimental Manual of Plant Biotechnology (edited by Watanabe andSugiura, Noson Bunka Publisher, 1989).

The probe to be used may be obtained by synthesizing DNA (with the chainlength of about 200 nucleotides to 500 nucleotides) having partialnucleotide sequences of the nucleotide sequence represented by SEQ IDNo: 1, 3 or 5 and labelling the DNA with radioisotope markers orfluorescent markers according to the known methods using, for example,Random Primed DNA Labelling Kit (Boehringer Co.), Random Primer DNALabelling Kit Ver. 2 (Takara Shuzo Co., Ltd.), ECL Direct Nucleic AcidLabelling and Detection System (Amersham Pharmacia Co.), MegaprimeDNA-labelling system (Amersham Pharmacia Co.) and the like.

Examples of the hybridization conditions include stringent conditionsand the following conditions may be exemplified: keeping at 65° C. inthe presence of 6×SSC (0.9 M NaCl and 0.09 M trisodium citrate),5×Denhard's solution [0.1% (w/v) ficoll 400, 0.1% (w/v)polyvinylpyrrolidone, 0.1% BSA], 0.5% (w/v) SDS and 100 ug/mldegenerated salmon sperm DNA or in DIG EASY Hyb solution(Boeringer-Mannheim Co.) containing 100 μg/ml of degenerated salmonsperm DNA, successively keeping at a room temperature for 15 minutes twotimes in the presence of 1×SSC (0.15 M NaCl and 0.015 M trisodiumcitrate) and 0.5% (w/v) SDS, and further keeping at 68° C. for 30minutes in the presence of 0.1×SSC (0.015 M NaCl and 0.0015 M trisodiumcitrate) and 0.5% SDS.

In order to obtain DNA coding the cytokinin receptor of Arabidopsis, PCRis carried out employing TAKARA LA TAQ™ (thermostable polymerase)(Takara Shuzo Co., Ltd.) and using a solution containing cDNA libraryphage of Arabidopsis (about 1,000,000 pfu) as a template and DNA havingthe nucleotide sequence represented by SEQ ID No: 11 and DNA having thenucleotide sequence represented by SEQ ID No: 12 as a primer set toamplify and obtain DNA to be a probe. The PCR solution to be used may beprepared by adding the reaction solutions instructed by the kit to 250ng of cDNA library.

The PCR conditions may be as follows: keeping at 94° C. for 2 minutes,at 8° C. for 3 minutes, and further repeating 40 cycles each of whichcomprises keeping at 94° C. for 30 seconds, at 55° C. for 30 seconds,and at 68° C. for 5 minutes.

Using the amplified and obtained DNA is used as a template, a32P-labeled probe may be produced employing Megaprime DNA-labelingsystem kit (Amersham Pharmacia Co.) and using the reaction solutionsinstructed by the kit. Using the probe obtained in such a manner, colonyhybridization is carried out by a conventional method, practically thehybridization is carried out keeping at 65° C. in the presence of 6×SSC(0.9 M NaCl and 0.09 M trisodium citrate), 5×Denhard's solution [0.1%(w/v) ficoll 400, 0.1% (w/v) polyvinylpyrrolidone, 0.1% BSA], 0.5% (w/v)SDS and 100 μg/ml degenerated salmon sperm DNA or in the DIG EASY Hybsolution (Boeringer-Mannheim Co.) containing 100 _(i)u , g/ml ofdegenerated salmon sperm DNA, successively keeping at a room temperaturefor 15 minutes two times in the presence of 1×SSC (0.15 M NaCl and 0.015M trisodium citrate) and 0.5% (w/v) SDS, and further keeping at 68° C.for 30 minutes in the presence of 0.1×SSC (0.015 M NaCl and 0.0015 Msodium citrate) and 0.5% SDS to obtain clone hybridized with the probe.

Further, DNA coding the cytokinin receptor may be prepared based on, forexample, the nucleotide sequence represented by SEQ ID No: 1, 3 or 5 bychemical synthesis of polynucleotides according to a common method suchas phosphite-triester method (Hunkapiller, M. et al., Nature, 310, 105,1984).

The DNA coding the cytokinin receptor obtained in such a manner may becloned in a vector by a common method described in, “Molecular Cloning:A Laboratory Manual 2nd edition” (1989), Cold Spring Harbor LaboratoryPress; “Current Protocols In Molecular Biology” (1987), John Wiley &Sons, Inc. ISBNO-471-50338-X, and the like. The vector to be used maybe, for example, pBlue Script II vector (produced by Stratagene Co.),pUC18/19 vector (produced by Takara Shuzo Co., Ltd.), TA cloning vector(produced by Invitrogen Co.), and the like.

Incidentally, the nucleotide sequence of cloned DNA may be confirmed by,the Maxam Gilbert method (described in, for example, Maxam, A., M & W.Gilbert, Proc. Natl. Acad. Sci. USA, 74, 560, 1977, and the like), theSanger method (described in, for example, Sanger, F. & A. R. Coulson, J.Mol. Biol., 94, 441, 1975, Sanger, F. & Nicklen and A. R. Coulson, Proc.Natl. Acd. Sci. USA, 74, 5463, 1977, and the like). For the process, thefollowing commercialized kits may be, for example, employed: ThermoSequenase II dye terminator cycle sequencing kit (produced by AmershamPharmacia Co.), Dye Terminator Cycle Sequencing FS Ready Reaction Kit(produced by PE Biosystems Japan Co.), and the like.

(3) Construction of Expression Vector

An expression vector of DNA coding the cytokinin receptor may beconstructed according to a common method described in, for example,Molecular Cloning 2nd edition written by J., Sambrook, E., F., Frisch, &T., Maniastis, published by Cold Spring Harbor Laboratory Press.

Usable are vectors to be used in host cells to be transformed, forexample, independently replicating vectors which contain geneticinformation possible to be duplicated in the host cells and further arepossible to be isolated from the host cells and purified and may havedetectable marker. More practically, in the case of using bacteria suchas E. coli as the host cells, for example, Plasmid pUC 119 (produced byTakara Shuzo Co., Ltd.), Phagemid pBluescript II (Stratagene Co.) andthe like may be used. In the case of using yeast as the host cells, forexample, Plasmid pACT2 (Clontech Co.) and the like may be used. In thecase of using plant cells as the host cells, for example, DNA coding thecytokinin receptor may be integrated with Plasmid pBI221 (Clontech Co.)to construct the vectors.

An expression vector possible to express DNA coding the cytokininreceptor in a host cell may be constructed by integrating a promoterwith the aforementioned vectors in the upstream of the DNA coding thecytokinin receptor in a binding manner of enabling to function in thehost cell. In this case, the phrase, “in a binding manner of enabling tofunction”, means that the promoter and the DNA coding the cytokininreceptor are bonded as to express the DNA coding the cytokinin receptorin the host cell under the control of the promoter. Usable as thepromoter possible to function in the host cell in the case of using E.coli as the host cell are, for example, a promoter (lacP) of lactoseoperon of E. coli, a promoter (trpP) of triptophan operon, a promoter(argP) of arginine operon, a promoter (galP) of galactose operon, atac-promoter, T7-promoter, T3-promoter, X-phage promoter, (X -pL, X-pR)and the like. In the case of using yeast as the host cell, it may beprepared by a conventional genetic engineering method [described inMethod in Enzymology 101 part (p. 192-201) by Ammerer, et. al.] fromADHI promoter (the ADHI promoter is available from the yeast expressionvector pAAH5 which contains the ADHI promoter and its terminator andwhich may be obtained from Washington Research Foundation). The ADHIpromoter is included in U.S. patent application No. 299,733 ofWashington Research Foundation and in the case that it is used forindustrial and commercial purposes in USA., it is required to obtainpermission from the patent holder. In the case of using a plant cell asthe host cell, usable examples are a nopaline synthesis enzyme gene(NOS) promoter, an octopine synthesis enzyme gene (OCT) promoter, acauliflower mosaic virus (CaMV)-derived 19S promoter, a CaMV-derived 35Spromoter and the like.

Further, in the case of integrating DNA coding the cytokinin receptorwith a vector previously having a promoter possible to function in ahost cell, DNA coding the cytokinin receptor is inserted in thedownstream of the promoter and the DNA coding the cytokinin receptor ina manner of enabling to function. For example, the aforementionedplasmid pACT 2 for yeast comprises the ADH1 promoter and therefore, anexpression vector possible to express the DNA coding the cytokininreceptor in yeast, for example, CG1945 (Clontech Co.) may be constructedby inserting the DNA coding the cytokinin receptor in the downstream ofthe ADH1 promoter of the plasmid pACT2.

(4) Production of Transformed Cell

A transformed cell to be used for the present invention may be producedby introducing the constructed expression vector into a host cell by aconventional method. As the host cell to be used for production of thetransformed cell, examples are bacteria, yeast, plant cell and the like.As bacteria, examples are bacteria belonging to E. coli, Serratia,Bacillus, Brevibacterium, Corynebacterium, Microbacterium and the like.As yeast, examples are budding yeast and fission yeast. Moreparticularly, examples are yeast belonging to Saccharomyces,Schizosaccharomyces and the like. As plant cell, examples are BY-2strain, which is a cultured cell of tobacco and BMS strain, which is acultured cell of corn (Black Mexican Sweet), and the like.

The method for introducing the expression vector into the aforementionedhost cell includes a conventional introduction method to be employedcorresponding to the host cell to be transformed. For example, in thecase of using bacteria as the host cell, the aforementioned expressionvector may be introduced into a host cell by employing a conventionalintroduction method such as a calcium chloride method and anelectroporation method described in, “Molecular Cloning” (by J.Sambrook, et. al, Cold Spring Harbor, 1989). In the case of using yeastas a host cell, the aforementioned expression vector may be introducedinto the host cell by employing Yeast transformation kit (produced byClontech Co.) based on a lithium method. Further, in the case of using aplant cell as a host cell, the aforementioned expression vector may beintroduced into the host cell by a conventional introduction method, forexample, Agrobacterium infection method (Japanese Examined PatentApplication No. 2 - 58917, Japanese Laid-Open Patent Application No.60-70080), an electroporation method into a protoplast (JapaneseLaid-Open Patent Application No. 60-251887, Japanese Laid-Open PatentApplication No. 5-68575), a particle gun method (Japanese Laid-OpenPatent Application No. 6-508316, Japanese Laid-Open Patent ApplicationNo. 63-258525).

(Transformed Cell in Which a Cytokinin Receptor of PartiallyTransmembrane Region-Deleted Type, i.e. a Cytokinin Receptor of aTransmembrane Time Variation Type, is Expressed.)

A cytokinin receptor to be used for the present invention includes acytokinin receptor wherein said cytokinin receptor has at least onetransmembrane region but less than that in its natural form (commonly 2to 4 transmembrane region) (incidentally, in the present invention, suchcytokinin receptors are sometimes referred to as cytokinin receptors ofpartially transmembrane region-deleted type). In this case, the phrase,“its natural form” means cytokinin receptors having an amino acidsequence most frequently existing among organisms having the similarnomenclature and generally called also as wild-type cytokinin receptor.

Such cytokinin receptors of partially transmembrane regions-deleted typeare cytokinin receptors whose transmembrane region structure may beassumed by employing structure assumption software and whosetransmembrane regions are partially deleted, for example, in 1 to 2sites and are less in number than the number of the transmembraneregions of the natural type cytokinin receptors (i.e. natural form).

More particularly, examples of such cytokinin receptors include acytokinin receptor having the amino acid sequence from amino acid number196 to 1176 among the amino acid sequence represented by SEQ ID No: 2 (2transmembrane regions); a cytokinin receptor having the amino acidsequence from amino acid number 50 to 1176 among the amino acid sequencerepresented by SEQ ID No: 2 (3 transmembrane regions); a cytokininreceptor having the amino acid sequence from amino acid number 32 to1036 among the amino acid sequence represented by SEQ ID No: 4 (3transmembrane regions); a cytokinin receptor having the amino acidsequence derived from the amino acid sequences of these cytokininreceptors wherein one or a plurality of amino acids are deleted,substituted or added, for example, cytokinin receptors having the aminoacid sequence derived from the amino acid sequences in which onemethionine is added to the amino-terminal and the like.

The DNA coding the cytokinin receptor may be constructed as to holdtransmembrane regions in a less number than the number of thetransmembrane regions of the natural type cytokinin receptors bypartially deleting the transmembrane regions by a conventional geneticengineering technique.

Production of the transformed cell in which the DNA coding the cytokininreceptor is introduced may be carried out according to theaforementioned method, “Production of transformed cell in which the DNAcoding a cytokinin receptor is introduced”.

(Transformed Cell to Express Chimera-Type Cytokinin Receptor)

A cytokinin receptor to be used in the present invention also includes achimera-type cytokinin receptor comprising extracellular regions of thecytokinin receptor, transmembrane regions of the cytokinin receptor, andhistidine kinase regions of the cytokinin receptor, wherein each of theregions is a homogeneous region to one another and receiver regions forthe histidine kinase, which are heterogeneous regions to these regions.

In the above, histidine kinase regions of the cytokinin receptor means,for example, a region existed at the C-terminal side of a transmembraneregion located in the N-terminal side of the cytokinin receptor, andsaid region having five conservative motifs which are common to generichistidine kinases as described in Annual Review of Genetics 23:311-336(1989), Microbiological Reviews 53(4):450-490 (1989), Science262:539-544 (1993), and the like. Examples of the region includes aregion having the amino acid sequence from amino acid number 587 to 844among the amino acid sequence represented by SEQ ID No: 2 in a case ofAHK2, a region having the amino acid sequence from amino acid number 450to 700 among the amino acid sequence represented by SEQ ID No: 4 in acase of AHK3 and a region having the amino acid sequence from amino acidnumber 449 to 714 among the amino acid sequence represented by SEQ IDNo: 6 in a case of CRE1.

Receiver regions of the cytokinin receptor means, for example, a regionexists between the histidine kinase region and the C-terminal end of thecytokinin receptor, and said region having three conservative motifswhich are common to generic histidine kinases as described in AnnualReview of Genetics 23:311-336 (1989), Science 262:539-544 (1993), andthe like. Examples of the region includes a region having the amino acidsequence from amino acid number 891 to 1163 among the amino acidsequence represented by SEQ ID No: 2 in a case of AHK2, a region havingthe amino acid sequence from amino acid number 746 to 1018 among theamino acid sequence represented by SEQ ID No: 4 in a case of AHK3 and aregion having the amino acid sequence from amino acid number 763 to 1038among the amino acid sequence represented by SEQ ID No: 6 in a case ofCRE1.

In addition, a sensor region for cytokinin means, for example, a regionwhich is a part of any of the extracellular regions of the cytokininreceptor, said region existed between a transmembrane region next to thehistidine kinase region and a transmembrane region secondary close tothe histidine kinase region, and said region have 50% and moreidentification and homology between three cytokinin receptors of AHK2,AHK3 and CRE1 as described in Plant and Cell Physiology 42(2):231-235(2001) and the like. Examples of the region includes a region having theamino acid sequence from amino acid number 259 to 536 among the aminoacid sequence represented by SEQ ID No: 2 in a case of AHK2, a regionhaving the amino acid sequence from amino acid number 120 to 399 amongthe amino acid sequence represented by SEQ ID No: 4 in a case of AHK3and a region having the amino acid sequence from amino acid number 132to 398 among the amino acid sequence represented by SEQ ID No: 6 in acase of CRE1.

The histidine kinase has the following sequence in common in plants,e.g. higher plants, and microorganism. That is, histidine kinase iscomposed of extracellular regions, transmembrane regions (generallyabout 2 to 4), histidine kinase regions having histidine kinase activityand holding histidine residue to be an active site, and receiver regionshaving a reception part for phosphate group transfer and holdingaspartic acid residue to be an active site. In the chimera-typecytokinin receptor, it is important that the extracellular regions,transmembrane regions, and histidine kinase regions are all derived fromthe same cytokinin receptor, whereas the receiver regions are deriveddifferently from the former cytokinin receptor.

It is sufficient for the receiver regions of the chimera-type cytokininreceptor to have a function of receiving signals transmitted from thehistidine kinase regions and transmitting them to the next step and anymay be usable as long as they can complement or improve the intrinsicfunctions of the receiver regions of histidine kinase comprising thehomogeneously derived extracellular regions, transmembrane regions, andhistidine kinase regions.

As such receiver regions, usable are, for example, receiver regions ofhistidine kinase derived from microorganism (e.g. receiver regions ofhistidine kinase derived from microorganism such as yeast, E. coli) andmore particularly receiver regions of histidine kinase coded in S1n1gene derived from budding yeast (e.g. the amino acid sequencerepresented by SEQ ID No: 7), receiver regions of histidine kinase codedin Chey gene derived from Salmonella, receiver regions of histidinekinase coded in RcsC gene, which is a hybrid sensor of E. coli [Maeda T,et al. Nature: 369 242-245, (1994): e.g. the amino acid sequencerepresented by SEQ ID No: 8], receiver regions of histidine kinase codedin Phks gene relevant to cell cycle control of fission yeast [Shieh, JC, et al., Gene Dev. 11, 1008-1022(1997)].

The DNA coding the chimera-type cytokinin receptor may be constructed byrespectively producing DNA for each of the extracellular regions of thecytokinin receptor, transmembrane regions of the cytokinin receptor,histidine kinase regions of the cytokinin receptor, and receiver regionsfor the histidine kinase, joining the DNA by a common geneticengineering technique so as to prevent appearance of any terminationcodon in the middle while using a proper linker so as to prevent frameshift. Incidentally, the DNA may be produced as one DNA fragment for theextracellular regions of the cytokinin receptor and transmembraneregions of the cytokinin receptor or for extracellular regions of thecytokinin receptor, transmembrane regions of the cytokinin receptor, andhistidine kinase regions of the cytokinin receptor.

The polynucleotides coding the aforementioned respective regions mayrespectively be produced by known methods. For example, in the case ofproduction by PCR, at first, the oligonucleotides (5′ side primers)having the nucleotide sequences of 5′ terminal regions of respectiveregions to be amplified and oligonucleotides (3′ side primers) havingcomplementary nucleotide sequences to the nucleotide sequences of 3′terminal are designed and synthesized. The primers may beoligonucleotides of about 14 nucleotides to about 35 nucleotides ingeneral and are preferable to contain restriction enzyme recognitionsequences usable at the time of ligating the polynucleotides amplifiedby the PCR to one another or these polynucleotides to vectors in the 5′side of the primers. Then, using the primers and the cDNA library as atemplate, amplification reactions may be carried out in the commonreaction conditions employed for the PCR. As the template to be used inthe case of producing the polynucleotides coding the extracellularregions through the transmembrane regions of the cytokinin receptor orthe histidine kinase regions of the cytokinin receptor, usable is cDNAlibrary derived from plants such as higher plants. Also as the templateto be used in the case of producing the polynucleotides coding thereceiver regions of the histidine kinase, usable is cDNA library derivedfrom microorganism prepared by a common method or the total DNA.

The production of the transformed cell in which the DNA coding thechimera-type cytokinin receptor is introduced may be carried outaccording to the aforementioned, “Production of the transformed cell inwhich the DNA coding a cytokinin receptor is introduced.”

(Intracellular Signal Transduction System Relevant to Cytokinin)

Measurement of the existence or the quantity of intracellular signaltransduction from the cytokinin receptor expressed in the transformedcell produced by the above-described manner in the present invention maybe carried out by utilizing the intracellular signal transduction systemwhich the host cell used for production of the transformed celloriginally has. The phrase, “ the existence or the quantity ofintracellular signal transduction” means, for example, the quantity ofthe cell growth of the transformed cell as an indicator. Alternatively,a regulator and/or a mediator having the intracellular signaltransduction function, so-called Two-Component regulatory system, isintroduced and expressed in the host cell and the expressed system maybe used as the intracellular signal transduction system. Usable as theTwo-Component regulatory system, for example, are Two-Componentregulatory systems corresponding to 5 types of ethylene receptors; ETR1,ETR2, ERS1, ERS2, and EIN4; which Arabidopsis has [Chang et al., Science262: 539-544 (1993), Hua et al., Science 269: 1712-1714 (1995), Sakai etal., Plant Cell Physiol 39: 1232-1239 (1998)] and AtHK1 having sensorfunctions to the osmotic pressure [Urao, Plant ell 11:1743-1754 (1999)].

As the host cell to be used for production of such a transformed cell,usable are host cells improved as to have histidine kinase activitylower than the intrinsic histidine kinase activity of the host cells.For example, it includes the host cells improved as to have histidinekinase activity lower than the intrinsic histidine kinase activity ofthe host cell by deleting one or more of histidine kinases. The phrase,“histidine kinase activity lower than” means that the quantity ofphosphate group transfer from histidine residue to be an active site ofhistidine kinase regions having histidine kinase activity to asparticacid residue to be an active site of receiver regions having a receptionpart has decreased. The state causes change of the quantity of the cellgrowth, change of the morphology, change of the shape, change of thequantity of the biosynthesis of specific compound, change of thequantity of the metabolism of specific compound in the transformed cellso improved as to have histidine kinase activity lower than theintrinsic histidine kinase activity of the host cell. More particularly,the following strain [Maeda T et al., Nature 369: 242-245 (1994)] may beexemplified: a strain obtained by defecting the S1n1 gene coding theprotein having the osmotic pressure sensor function and derived from thebudding yeast such as Saccharomyces cerevisiae and the like. Since thestrain has decreased quantity of the cell growth in the cause of beingdefected in the histidine kinase existing in Saccharomyces cerevisiae,it can more clearly detect the existence or the quantity of theintracellular signal transduction from the cytokinin receptor expressedin the transformed cell by using the quantity of the cell growth of thetransformed cell as an indicator. Further, other preferable examplesincludes a defective strain of the RcsC gene, which is a hybrid sensorderived from E. coli and a defective strain of Phks gene relevant to thecell cycle control of fission yeast.

(Method for Analyzing Agonist-Activity and Antagonist-Activity to aCytokinin Receptor)

In the method for analyzing agonist-activity to a cytokinin receptor,examples of the first step of bringing an examinee substance intocontact with a transformed cell into which DNA coding the cytokininreceptor is introduced include a method for culturing the transformedcell in a culture medium containing the examinee substance. In order toculture the transformed cell, both cultures are usable: liquid-phaseculture for culturing the transformed cell in a liquid culture mediumand a solid-phase culture for culturing the transformed cell in a solidculture medium produced by adding agar or the like to the liquid culturemedium. The concentration of an examinee substance in the culture mediumis about 1 nM to about 1 mM and preferably about 10 nM to about 100 μM.The culture time is, for example, 1 hour or longer and 3 days andpreferably 25 hours to 2 days. Incidentally, in the case of method foranalyzing the agonist-activity to the cytokinin receptor, the culturecontaining no cytokinin may be used as the culture containing theexaminee substance.

In the method for analyzing the antagonist-activity to the cytokininreceptor, examples of the first step of bringing an examinee substanceand a substance having the agonist-activity to the cytokinin receptorinto contact with a transformed cell into which DNA coding the cytokininreceptor is introduced include a method for culturing the transformedcell in a culture medium containing the examinee substance and asubstance having the agonist-activity to the cytokinin receptor. Inorder to culture the transformed cell, both cultures are usable:liquid-phase culture for culturing the transformed cell in a liquidculture medium and a solid-phase culture for culturing the transformedcell in a solid culture medium produced by adding agar or the like tothe liquid culture medium. The concentration of an examinee substance inthe culture medium is about 1 nM to about 1 mM and preferably about 10nM to about 100 μM. The concentration of the substance (e.g. cytokininssuch as trans-zeatin, cis-zeatin, benzyl adenine, thidiazuron and thelike) having the agonist-activity to the cytokinin receptor is about 1nM to about 1 mM and preferably about 10 nM to about 100 μM. The culturetime is, for example, 1 hour or longer and 3 days and preferably 25hours to 2 days. Incidentally, in the case of method for analyzing theagonist-activity to the cytokinin receptor, the culture containing nocytokinin may be used as the culture containing the examinee substance.

The agonist-activity or the antagonist-activity of an examinee substanceto the cytokinin receptor may be detected by evaluating theagonist-activity of two or more different examinee substances to thecytokinin receptor based on the difference obtained by comparison of theexistence and the quantity of the intracellular signal transduction in aresion where the examinee substances (preferable is, for example,between at least two or more different examinee substances, at least onehas no agonist-activity or antagonist-activity to the cytokininreceptor) are independently used and measured by the aforementionedmethod for analyzing the agonist-activity or the antagonist-activity tothe cytokinin receptor.

More particularly, for example, in the case of using a transformed cell(that is, a transformed cell having a function of directly controllingthe cell growth by intracellular signal transduction from the cytokininreceptor) produced using TM182 (S1n1 Δ) [Maeda T et al, Nature 369:242-245 (1994)], a S1n1 genetically defected strain in which, forexample, PTP2 Tyrosine phosphatase gene [Ota et al. Proc. N. A. Sci.,USA, 89, 2355-2359 (1992)] is introduced as a host cell, theagonist-activity to the cytokinin receptor may be measured using, as anindicator, the quantity of the cell growth of the transformed cell in aculture medium (an agar culture medium or a liquid culture medium)containing glucose as a carbon source, for example, a DOLU−Gul culturemedium. In this case, if into the DOLU+Gul culture medium is added theexaminee substance and no substance having the agonist-activity to thecytokinin receptor, the examinee substance found capable of growing thetransformed cell can be evaluated as a substance having theagonist-activity to the cytokinin receptor. On the other hand, if intothe DOLU+GUL culture medium is added the examinee substance and asubstance having the agonist-activity to the cytokinin receptor, theexaminee substance found capable of suppressing or inhibiting the growthof the transformed cell can be evaluated as a substance having theantagonist-activity to the cytokinin receptor.

Incidentally, as a blank, investigation may be carried out to find thegrowth of the transformed cell in a culture medium using galactose asthe carbon source in place of glucose, for example, a DOLU+Gal culturemedium, independently of the existence of the examinee substance.

Further, in the case of using a transformed cell produced by employingfission yeast, which is a Phks genetically defected strain, as a hostcell (that is, a transformed cell having a function of directlycontrolling the cell growth by the intracellular signal transductionfrom the cytokinin receptor), the fission pattern of the fission yeastmay be observed with a microscope. In this case, if the culture mediumcontains the examinee substance and no substance having theagonist-activity to the cytokinin receptor, the examinee substance foundcapable of normal fission and propagation of the transformed cell can beevaluated as a substance having the agonist-activity to the cytokininreceptor. On the other hand, if the culture medium contains an examineesubstance and a substance having the agonist-activity to the cytokininreceptor, the examinee substance found capable of suppressing orinhibiting the normal fission and propagation of the transformed cellcan be evaluated as a substance having the antagonist-activity to thecytokinin receptor.

Furthermore, in the case of using a transformed cell produced byemploying E. coli defective in RcsC gene into which cps-LacZ isintroduced as a host cell (that is, a transformed cell having a functionof directly controlling reporter gene expression by the intracellularsignal transduction from the cytokinin receptor), the X-Gal coloring maybe observed in an agar culture medium or a liquid culture medium [Suzukiet al. Plant Cell Physiol 42: 107-113 (2001)]. In this case, if theculture medium contains the examinee substance and no substance havingthe agonist-activity to the cytokinin receptor, the examinee substancefound capable of coloring the transformed cell to be blue can beevaluated as a substance having the agonist-activity to the cytokininreceptor. On the other hand, if the culture medium contains the examineesubstance and a substance having the agonist-activity to the cytokininreceptor, the examinee substance found capable of disappearing coloringthe blue of the transformed cell can be evaluated as a substance havingthe antagonist-activity to the cytokinin receptor.

Moreover, an agonist-active substance or an antagonist-active substanceto the cytokinin receptor may be searched by selecting substances havingthe agonist-active substance or the antagonist-active substance to thecytokinin receptor based on the agonist-activity or theantagonist-activity to the cytokinin receptor evaluated by theaforementioned detection methods.

Further, a substance selected by the above described detection methodsmay be utilized as an active ingredient of a plant growth regulator.

The plants to be the objects to be treated with the aforementioned plantgrowth regulator are, for example, decorative plants such as floweringplants and ornamental foliage plants; cultivating plants such as crop,vegetable, fruit and the like; fibrous plants; trees; lawn and the like.

The growth regulator is generally mixed with a solid carrier, a liquidcarrier, and the like and further, if needed, mixed with a surfactantand other auxiliary agents for the formulation of an agricultural andhorticultural agent and formulated in an emulsion agent, a hydratingagent, a suspension agent, a solution agent and the like. In theseagricultural and horticultural agents, an agonist-active substance or anantagonist-active substance to the cytokinin receptor may be containedgenerally in 0.5 to 90% by weight and preferably in 1 to 80% by weight.

Usable as the solid carrier to be used for the formulation of anagricultural and horticultural agent are, for example, clays (kaolinite,kieselguhr, synthesized hydrated silicon oxide, intercalated clays,bentonite, acidic white clay, and the like), talc, other inorganicminerals (sericite, quartz powder, sulfur powder, activated carbon,calcium carbonate, and the like), chemical fertilizers (ammoniumsulfate, ammonium phosphate, ammonium nitrate, ammonium chloride, urea,and the like) in finely powdered state or in granular state and usableas the liquid carrier are, for example, water, alcohols (methanol,ethanol and the like), ketones (acetone, methyl ethyl ketone,cylohexanone and the like), aromatic hydrocarbons (toluene, xylene,ethylbenzene, methylnaphthalene and the like), non-aromatic hydrocarbons(hexane, cyclohexane, kerosene and the like), esters (ethyl acetate,butyl acetate and the like), nitriles (actonitrile, isobutylnitrile andthe like), ethers (dioxane, diisopropyl ether and the like), acid amides(dimethylformamide, dimethylacetamide and the like), halohydrocarbons(dichloroethane, trichloroethane and the like), etc.

As the surfactant, usable are, for example, alkylsulfuric acid esters,alkylsulfonic acid salts, alkylarylsulfonic acid salts, alkylaryl ethersand their polyoxyethylene compounds, polyethylene glycols, polyhydricalcohol esters, sugaralcohols and the like.

As other auxiliary agents for the formulation of agricultural andhorticultural agents, usable are solidification agents and dispersanstsuch as casein, gelatin, polysaccharides (starch, acacia, cellulosederivatives, alginic acid and the like), lignin derivatives, bentonite,synthesized water-soluble polymer [poly(vinyl alcohol), poly(vinylpyrolidone), poly(acrylic acid) and the like] and the like, andstabilizers such as PAP (acidic isopropyl phosphate), BHT(2,6-tert-butyl-4-methylphenol), BHA (2-/3-tert-butyl-4-methoxyphenol),plant oils, mineral oils, aliphatic acids, aliphatic acid esters and thelike.

The agonist-active substance or the antagonist-active substance to thecytokinin receptor made to be agricultural and horticultural agents isused as it is or diluted with water to carry out treatment for the stemand leave parts, branch and leave parts, and flower and fruit parts ofplants by spraying, for fruits by immersion, and for fruits byapplication. The plant growth regulator is used for the object plants tocarry out the treatment once or a plurality of times.

In the case of using the plant growth regulator for the purpose ofsuppressing the dropping of fruits, the plant growth regulator isdiluted with water and the resulting diluted agent is sprayed to thefruit parts and branch and leave parts before harvest.

In the case of using the plant growth regulator for the purpose ofsuppressing the ball dropping of cotton, the plant growth regulator isdiluted with water and the resulting diluted agent is sprayed to theballs and stem and leave parts of cotton before harvest.

The plant growth regulator may be used for the treatment of growingplants or of plants after harvest.

The application amount of the agonist-active substance or theantagonist-active substance to the cytokinin receptor in an agriculturaland horticultural agent is generally 1 to 8000 g per 1 hectare, althoughit is changed depending on the state of the agricultural andhorticultural agent, the timing for the treatment, the method for thetreatment, the site for the treatment, and the object plant to betreated. Also in the case of using the plant growth regulator whilediluting the agent with water, the concentration of the agent isgenerally 0.0001 to 1000 mM and preferably 0.001 to 10 mM, although itis changed depending on the state of the agricultural and horticulturalagent, the timing for the treatment, the method for the treatment, thesite for the treatment, and the object plant to be treated.

Next, hereinafter given are formulation examples of an agricultural andhorticultural agent produced from an agonist-active substance or anantagonist-active substance to the cytokinin receptor and used as aplant growth regulator. The parts in the following description of theexamples denotes the parts by weight.

FORMULATION EXAMPLE 1

A hydrating agent was obtained by sufficiently pulverizing and mixing 50parts of an agonist-active substance or an antagonist-active substanceto the cytokinin receptor, 3 parts of calcium ligninsulfonate, 2 partsof sodium laurylsulfate, and 45 parts of synthesized hydrated siliconoxide.

FORMULATION EXAMPLE 2

A hydrating agent was obtained by sufficiently pulverizing and mixing 70parts of an agonist-active substance or an antagonist-active substanceto the cytokinin receptor, 3 parts of calcium ligninsulfonate, 2 partsof sodium laurylsulfate, and 25 parts of synthesized hydrated siliconoxide.

FORMULATION EXAMPLE 3

An emulsion agent was obtained by mixing 40 parts of an agonist-activesubstance or an antagonist-active substance to the cytokinin receptor, 3parts of polyoxyethylene sorbitane monoolate, 2 parts of CMC(carboxymethyl cellulose), and 52 parts of water and wet-pulverizing theresultant mixture to be 5 μm or smaller in the particle size.

The present invention makes it possible to analyze the agonist-activityand the antagonist-activity to the cytokinin receptor and also makes itpossible to quickly search the substances having the agonist-activityand the antagonist-activity to the cytokinin receptor even in a smallamount of examinee substances by employing the analysis method.

EXAMPLES

Hereinafter, although the present invention will be described in detailwith the reference to examples, the present invention is not at allrestricted to these examples.

Example 1 Production of Arabidopsis cDNA Phage Library for CRE1 Cloning

Seeds of Arabidopsis thaliana ecotype Wassilewskija were sterilized with70% of ethyl alcohol for 1 minute and further sterilized with 1.5% ofsodium hypochlorite for 10 minutes. The resulting seeds were well washedwith sterilized water and then cultured for 2 weeks in GM culture medium[4.3 g Murashige and Skoog's basal salt mixture, 1% sucrose, 10 ml of 5%MES-KOH (pH 5.7), 0.3% PHYTAGEL™ (gellan gum) (SIGMA)] to obtain 5 g ofthe plant. After the plant was frozen in liquified nitrogen andphysically milled with a mortar and a pestle. The resulting milledproduct was mixed with a mixed solution of 10 ml of an extraction buffer[200 mM Tris-HCl (pH 8.5), 100 mM NaCl, 10 mM EDTA, 0.5% SDS, 14 mM(3-mercaptoethanol] and 10 g of phenol. After being mixed by a Voltexmixer, the resulting mixture was mixed further with 10 ml of chloroformand vigorously stirred and subjected to centrifugal separation at 10,000rotation for 20 minutes. The recovered aqueous layer was mixed with LiClin the concentration to be 2M of the final concentration, left still at-80° C. for 3 hours, thawed and subjected to centrifugal separation at10,000 rotation for 20 minutes to recover a precipitate. The recoveredprecipitate was dissolved in 2 ml of TE [10 mM Tris-HCl (pH 8.0), 1 mMEDTA] and then further mixed with 0.2 ml of 3 M sodium acetate (pH 5.2)and 5 ml ethanol and subjected to centrifugal separation to recover RNAas a precipitate. Further, the precipitate (RNA) was subjected totreatment with OLIGOTEX™ dt30 super (oligo d(T) latex beads) (NipponRosch Co.) to extract RNA integrated with polyA.

The production of phage cDNA library from the extracted RNA integratedwith polyA was carried out employing ZAP-cDNAR Synthesis Kit (StratageneCo.) according to the instruction. The potency of the produced phagecDNA library was 500,000 PFU.

Example 2 Production of DNA Probe of CRE1

The PCR was carried out employing TAKARA LA Taq™ (Takara Shuzo Co.,Ltd.) and using a phage solution (about 1,000,000 PFU) of the phage cDNAlibrary produced in the example 1 as a template and DNA having thenucleotide sequence represented by SEQ ID No: 11 and DNA having thenucleotide sequence represented by SEQ ID No: 12 as the primers toamplify DNA. The procedure will be described in detail below.

A PCR solution was prepared by adding a reaction composition containingdNTP and the like to the phage 1,000,000 pft and respective primer DNAeach in 0.2 μM according to the instruction of the kit and the desiredDNA flagment was amplified in PCR conditions: keeping at 94° C. for 2minutes, and further repeating 40 cycles each of which comprised keepingat 94° C. for 30 seconds, at 55° C. for 30 seconds, and at 68° C. for 5minutes. Next, using the amplified DNA flagment as a template, a probelabelled with 32P was prepared employing Megaprime DNA-labelling systemkit (Amersham Pharmacia Co.). Incidentally, reaction solution (25 μl wasprepared by adding 2.0 MBq of 32P dCTP to 25 ng of amplified DNAflagment and adding a reaction composition instructed by the kit. Thelabelling reaction was carried out at 37° C. for 10 minutes.

Example 3 Production of Phage cDNA Clone Holding CRE1

The cloning of desired CRE1 gene was carried out by plaque hybridizationusing the probe prepared by the example 1. Detailed description will begiven below.

Using the phage cDNA library produced in the example 1 and according tothe instruction of ZAP-cDNAR Synthesis Kit, plaque was produced. DNA wasadsorbed on a nitrocellulose filter from the produced plaque and thentreated with UV rays to be fixed on the filter. Using the filterprepared in such a manner, hybridized phage cDNA clone was obtained bykeeping at 65° C. in the presence of 6×SSC (0.9 M NaCl and 0.09 Mtrisodium citrate), 5×Denhard's solution [0.1% (w/v) ficoll 400, 0.1%(w/v) polyvinylpyrrolidone, 0.1% BSA], 0.5% (w/v) SDS and 100 μg/mldegenerated salmon sperm DNA or in DIG EASY Hyb solution(Boeringer-Mannheim Co.) containing 100 μg/ml of degenerated salmonsperm DNA, successively keeping at a room temperature for 15 minutes twotimes in the presence of 1×SSC (0.15 M NaCl and 0.015 M trisodiumcitrate) and 0.5% (w/v) SDS, and further keeping at 68° C. for 30minutes in the presence of 0.1×SSC (0.015 M NaCl and 0.0015 M trisodiumcitrate) and 0.5% SDS.

Example 4 Cloning of CRE1 cDNA

Using the cDNA of the phage cDNA clone obtained by the example 3 as atemplate and DNA having the nucleotide sequence represented by SEQ IDNo: 13 and DNA represented by SEQ ID No: 14 as primers, DNA having thenucleotide sequence represented by SEQ ID No: 5 was amplified by PCR.Detailed description will be given below.

The PCR was carried out employing Herculase Enhanced DNA Polymerase(TOYOBO Co., Ltd.) in the reaction conditions of keeping at 94° C. for 1minute, and further repeating 25 cycles each of which comprised keepingat 94° C. for 30 seconds, at 55° C. for 30 seconds, and at 72° C. for 4minutes. Incidentally, the PCR solution (50 μl) was prepared by adding areaction composition containing dNTP and the like to 500 ng of cDNA ofthe phage cDNA clone and respective primer DNA each in 100 ng accordingto the instruction of the kit.

The desired DNA flagment was amplified in such a manner.

Example 5 Construction of CRE1 Expression Vector

After p415CYC1, a yeast expression vector, [Munberg et al. Gene: 156119-122 (1995), available from ATCC library (No. 873821)] was digestedwith a restriction enzyme Sma I and then using T4 DNA ligase, DNA havingthe nucleotide sequence represented by SEQ ID No: 5 and obtained by theexample 3 was ligated downstream of the CYC 1 promoter sequence of theexpression vector p415CYC1 as to be integrated to express the desiredprotein in yeast. The constructed DNA was confirmed to be in the rightdirection and its nucleotide sequence was confirmed to be the nucleotidesequence represented by SEQ ID No: 6 by an automatic DNA sequencer andthen the expression plasmid p415CYC-CRE 1 was obtained.

Example 6 Cloning of AHK3 (AAF99730) cDNA

Seeds of Arabidopsis thaliana ecotype Wassilewskija were sterilized with70% of ethyl alcohol for 1 minute and further sterilized with 1.5% ofsodium hypochlorite for 10 minutes. The resulting seeds were well washedwith sterilized water and then cultured for 2 weeks in GM culture medium[4.3 g Murashige and Skoog's basal salt mixture, 1% sucrose, 10 ml of 5%MES-KOH (pH 5.7), 0.3% PHYTAGEL™ (gellan gum) (SIGMA)] to obtain 5 g ofthe plant. After the plant was frozen in liquified nitrogen andphysically milled with a mortar and a pestle. The resulting milledproduct was mixed with a mixed solution of 10 ml of an extraction buffer[200 mM Tris-HCl (pH 8.5), 100 mM NaCl, 10 mM EDTA, 0.5% SDS, 14 mMβ-mercaptoethanol] and 10 g of phenol. After being mixed by a Voltexmixer, the resulting mixture was mixed further with 10 ml of chloroformand vigorously stirred and subjected to centrifugal separation at 10,000rotation for 20 minutes. The recovered aqueous layer was mixed with LiClin the concentration to be 2M of the final concentration, left stillat−80° C. for 3 hours, thawed and subjected to centrifugal separation at10,000 rotation for 20 minutes to recover a precipitate. The recoveredprecipitate was dissolved in 2 ml of TE [10 mM Tris-HCl (pH 8.0), 1 mMEDTA] and then further mixed with 0.2 ml of 3 M sodium acetate (pH 5.2)and 5 ml ethanol and subjected to centrifugal separation to recover RNAas a precipitate. Further, 40 μg of the precipitate (RNA) was mixed with30 unit of FPLC pure™ Dnasel I (RNase free-DNase I) (Amersham-Pharmacia)and 60 unit of Superace (Ambion) to remove mixed genome DNA and theresulting RNA was subjected to the phenol/chloroform treatment andethanol treatment to purify the RNA. Next, using the purified RNA as atemplate and oligo (dT) 12-18 (Amersham-Pharmacia) as a primer, RT-PCRwas carried out. The RT-PCR was carried out employing Superscript II(GIBCO BRL Co.) at 42° C. for 40 minutes. Incidentally the PT-PCRsolution was prepared according to the method described in instructionof the Superscript II.

The desired cDNA was amplified in such a manner.

Using the amplified cDNA as a template and DNA having the nucleotidesequence represented by SEQ ID No: 16 and DNA having the nucleotidesequence represented by SEQ ID No: 17 as primers, DNA having thenucleotide sequence represented by SEQ ID No: 3 was amplified by PCR.The PCR was carried out using Herculase Enhanced DNA Polymerase (TOYOBOCo., Ltd.) in the reaction conditions of keeping at 94° C. for 1 minute,and further repeating 41 cycles each of which comprised keeping at 94°C. for 30 seconds, at 55° C. for 30 seconds, and at 72° C. for 4 minute.Incidentally, the PCR solution (50 μ) was prepared by adding a reactioncomposition containing dNTP and the like to 500 ng of the template DNAand respective primer DNA each in 100 ng according to the instruction ofthe kit.

The desired DNA fragment was amplified in such a manner.

Example 7 Construction of pHM-1

After p415CYC1 Nunberg et al. Gene: 156 119-122 (1995); available fromATCC library (No. 87382)] was digested with the restriction enzyme Spe Iand BamH I, synthesized DNA flagments (linkers) having the nucleotidesequence represented by SEQ ID Nos: 18 and 15 were inserted to theexpression vector p415CTC1 using T4 DNA ligaseas to newly add therestriction enzyme sites Sac II, Apa I, Nhe Ito the plasmid p415CYC1 andconstruct pHM-1.

Example 8 Construction of AHK3 Expression Vector

After the pHM-1 was digested with the restriction enzyme Sal I and SacII, and then using T4 DNA ligase, DNA having the nucleotide sequencerepresented by SEQ ID No: 3 was introduced downstream of the CYC1promoter sequence of the expression vector pHM-1 as to be integrated toexpress the desired protein in yeast. The constructed DNA was confirmedto be right in the direction and its nucleotide sequence was confirmedto be right in the sequence by an automatic DNA sequencer and thus theexpression plasmid p415CYC-AHK3 was obtained.

Example 9 Cloning of AHK2(BAB09274)cDNA

Using the DNA fragments obtained by the example 6 (the cDNA prepared byreverse transcription of the total RNA) as a template and DNA having thenucleotide sequence represented by SEQ ID No: 19 and DNA having thenucleotide sequence represented by SEQ ID No: 20 as primers, DNA havingthe nucleotide sequence represented by SEQ ID No: 1 was amplified byPCR. The PCR was carried out employing TAKARA Pfu Turbo denature (TakaraShuzo Co., Ltd.) in the reaction conditions of keeping at 94° C. for 1minute, and further repeating 30 cycles each of which comprised keepingat 94° C. for 30 seconds, at 55° C. for 30 seconds, and at 72° C. for 4minutes. Incidentally, the PCR solution (50 μl) was prepared by adding areaction composition containing dNTP and the like to 500 ng of thetemplate DNA and respective primer DNA each in 50 ng according to theinstruction of the kit.

The desired DNA flagment was amplified in such a manner.

Example 10 Cloning of AHK2(BAB09274) ΔcDNA

Using the DNA flagments obtained by the example 6 (the cDNA prepared byreverse transcription of the total RNA) as a template and DNA having thenucleotide sequence represented by SEQ ID No: 21 and DNA having thenucleotide sequence represented by SEQ ID No: 22 as primers, PCR wascarried out to amplify DNA having the nucleotide sequence represented bySEQ ID No: 1 in which ATG was added to the 5′ terminal sites of thenucleotide sequence from the nucleotide numbers 586 to 3531. The PCR wascarried out employing TAKARA Pfu Turbo denature (Takara Shuzo Co., Ltd.)in the reaction conditions of keeping at 94° C. for 1 minute, andfurther repeating 30 cycles each of which comprised keeping at 94° C.for 30 seconds, at 55° C. for 30 seconds, and at 72° C. for 4 minutes.Incidentally, the PCR solution (50 μl) was prepared by adding a reactioncomposition containing dNTP and the like to 500 ng of the template DNAand respective primer DNA each in 50 ng according to the instruction ofthe kit.

The desired DNA flagment was amplified in such a manner.

Example 11 Construction of AHK2 and AHK2 Δ Expression Vector

After pHM-1 was digested with a restriction enzyme Sac II and Nhe I andthen using T4 DNA ligase, DNA flagments obtained by the example 9 andthe example 10 were respectively ligated downstream of the CYC 1promoter sequence of the expression vector pHM-1 as to be integrated toexpress the desired protein in yeast. The introduced DNA was confirmedto be right in the direction and its nucleotide sequence was confirmedto be right in the sequence by an automatic DNA sequencer and thus theexpression plasmid p415CYC-AHK 2 and p415CYC-AHK2 Δ were obtained.

Example 12 Production of Transformed Cells TM182-CRE1, TM182-AHK2,TM182-AHK2 Δ and TM182-AHK3

Transformation of TM182 (S1n1 Δ), S1n1 genetically detected strain,[Maeda T et al. Nature: 369 242-245 (1994)] was carried out using theobtained expression plasmid p415CYC-CRE1 (the example 5), p415CYC-AHK2(the example 11), p415CYC-AHK2Δ (the example 11) and p415CYC-AHK3 (theexample 8). The transformation was carried out by employing Polyethyleneglycol/lithium acetate (PEG/LiAc)-mediated transformation methodaccording to the description of VII. Library Transformation & ScreeningProtocols disclosed in MATCHAMAKER Two-Hybrid System 3 User Manual p. 22from CLONTECH Co. Transformed cells TM182-CRE1, TM182-AHK2, TM182-AHK2 Δand TM182-AHK3 were produced by selecting in the DOLU+Gal culture mediumbased on disappearance of leucine nutrient requirement in thetransformed cell.

Example 13 Response of Transformed Cells TM182-CRE1, TM182-AHK2,TM182-AHK2 Δ and TM182-AHK3 to Cytokinin (Part 1)

A culture solution 10 μl (about 800 clones of yeast) of the transformedcells TM182-CRE1, TM182-AHK2, TM182-AHK2 0 and TM182-AHK3 produced bythe example 12 was spotted on DOLU+Gul agar media containing 10 μM oftrans-zeatin and cultured at 30° C. for 30 hours. After incubation, thegrowth state of the transformed cells was observed and photographed by adigital camera.

As a result, any of the transformed cells TM182-CRE1, TM182-AHK2,TM182-AHK2 Δ and TM182-AHK3 showed high growth in the case of using theDOLU+Gul agar culture media containing trans-zeatin as compared withthat in the case of using the DOLU+Gul agar culture media containing notrans-zeatin. The results showed that the transformed cells responded tocytokinin and that they were possible to be grown in the DOLU+Gul agarculture media. Further the transformed cells were found possible to begrown in the DOLU+Gal agar culture media independently of the existencetrans-zeatin.

Example 14 Response of Transformed Cells TM182-CRE1, TM182-AHK2 Δ andTM182-AHK2 to Cytokinin (Part 2)

Culture solutions of the transformed cells TM182-CRE1, TM182-AHK2 Δ, andTM182-AHK2 produced by the example 12 were spotted on DOLU+Gul agarmedia containing cytokinin in a variety of concentrations (1 nM, 10 nM,100 nM, 1 μM, 10 μM, 100 μM) and cultured at 30° C. for 30 hours. Afterincubation, the growth state of the transformed cells was observed andphotographed by a digital camera.

The lowest supply concentrations of trans-zeatin and cis-zeatin in whichthe respective transformed cells could be grown were shown in Table 1.

TABLE 1 cytokinin TM182-CRE1 TM182-AHK2 TM182-AHK2 A trans-zeatin 10 μM 1 μM 100 nM cis-zeatin no growth 10 μM 1 μM

Example 15 Method for Searching Substance having Aagonist-Activity toCytokinin Receptor (Part 1)

The transformed cells TM182-CRE1, TM182-AHK2, TM182-AHK2 Δ andTM182-AHK3 produced in the example 12 were inoculated in 200 ml ofDOLU+Gal culture media and pre-cultured at 30° C. for 36 hours. Thepre-cultured solutions were diluted with DOLU+Gul media as to become0.100 as the optical density (0D₆₀₀) and further the resultants werediluted with DOLU+Gul media at a dilution rate of 1/200 to obtaindiluted pre-cultured solutions.

An assay plate was prepared by filling respective wells of a 96-wellplate with 20 μl of solutions which were prepared by diluting DMSOsolution (10 mM) of each examinee substance with DOLU+Gul medium at adilution rate of 1/100, said solutions containing each examineesubstance to be 100 μM at the final concentration. Simultaneously, anassay plate only filled with 20 μl of solutions which were prepared bydiluting DMSO solution with DOLU+Gul medium, said solutions containingno examinee substance, was prepared as the blank sections.

The diluted pre-cultured solutions were added in 200 μl each into therespective wells of both assay plates and cultured at 30° C. for 24hours and then the optical density (0D₆₂₀) of each well was measured bya plate reader. The agonist-activity of the examinee substances to thecytokinin receptor was detected by comparing the optical densitymeasured in the testing sections to which the examinee substances wereadded with the optical density measured in the blank sections. Theoptical density of the culture solutions of the transformed cells in thetesting sections to which the examinee substances were added were shownin Table 2. Compound B showing the higher optical density measured inthe testing sections to which the examinee substances were added thanthat in the blank sections were selected as agonist-active substance tothe cytokinin receptor.

TABLE 2 Examinee substance TM182-AHK2 TM182-AHK2 Δ TM182-AHK3 DMSO 0.010 0.51 Compound A^(*1) 0.01 0 0.54 Compound B^(*2) 0.45 0.89 0.88^(*1)Abscisic acid (=negative control) ^(*2)6-Benzyl aminopurine(=positive control)

Example 16 Method for Searching Substance having Antagonist-Activity toCytokinin Receptor (Part 2)

The transformed cells TM182-CRE1, TM182-AHK2, TM182-AHK2 Δ andTM182-AHK3 produced in the example 12 were inoculated in 200 ml ofDOLU+Gal culture media and cultured at 30° C. for 30 hours to obtainpre-cultured solutions.

An assay plate is prepared by filling respective wells of a 96-wellplate with 200 μl of each DOLU+Gul medium mixed with 1 μM oftrans-zeatin (cytokinin), and into the assay plate is put each examineesubstance to be 1 μM at the final concentration. Simultaneously, anassay plate only filled with 200 μl of the DOLU+Gal medium mixed with 1μM of trans-zeatin is prepared as the blank sections.

The pre-cultured solutions are added in 20 μl each into the respectivewells of both assay plates and cultured at 30° C. for 30 hours and thenthe optical density of each well is measured by a plate reader. Theantagonist-activity of the examinee substances to the cytokinin receptoris detected by comparing the optical density measured in the testingsection to which the examinee substances are added with the opticaldensity measured in the blank sections. The examinee substances showingthe lower optical density measured in the testing sections to which theexaminee substances are added than that in the blank sections areselected as antagonist-active substance to the cytokinin receptor.

Example 17 Method for Searching Substance having Agonist-Activity toCytokinin Receptor (Part 3)

The transformed cells TM182-CRE1, TM182-AHK2, TM182-AHK2 Δ andTM182-AHK3 produced in the example 12 were inoculated in 200 ml ofDOLU+Gal culture media and cultured at 30° C. for 30 hours to obtainpre-cultured solutions.

The pre-cultured transformed cells (TM182-CRE1, TM182-AHK2, TM182-AHK2 Δand TM182-AHK3) are spot-added in 10 μl to the respective DOLU+Gul agarculture media to which agonist-active substances to the cytokininreceptor selected by the example 15 are added while their concentrationbeing changed from 10 nM to 100 μM and then is cultured at 30° C. for 30hours. After incubation, the intensity of the agonist-activity of theexaminee substances to the cytokinin receptor is detected and confirmedbased on the lowest concentration at which transformed cells(TM182-CRE1, TM182-AHK2, TM182-AHK2 Δ and TM182-AHK3) are observed togrow.

Example 18 Method for Searching Substance having Antagonist-Activity toCytokinin Receptor (Part 4)

The transformed cells TM182-CRE1, TM182-AHK2, TM182-AHK2 Δ andTM182-AHK3 produced in the example 12 are inoculated in 200 ml ofDOLU+Gal culture media and cultured at 30° C. for 30 hours to obtainpre-cultured solutions.

The pre-cultured transformed cells (TM182-CRE1, TM182-AHK2, TM182-AHK2 Δand TM182-AHK3) are spot-added in 10 μl to the respective DOLU+Gul agarculture media to which antagonist-active substances to the cytokininreceptor selected by the example 16 are added while their concentrationbeing changed from 10 nM to 100 μM and also 10 μM of trans-zeatin(cytokinin) is added and then is cultured at 30° C. for 30 hours. Afterincubation, the intensity of the antagonist-activity of the examineesubstances to the cytokinin receptor is detected and confirmed based onthe lowest concentration at which transformed cells (TM182-CRE1,TM182-AHK2, TM182-AHK2 Δ and TM182-AHK3) are not observed to grow.

Hereinafter, the medium compositions to be used in the present inventionwill be described:

-   (a) DOLU+GLU culture medium

Bacto-yeast nitrogen base without amino acids 6.7 g Glucose 20 gDrop-out mix (x) 2.0 g Distilled water 1000 ml

-   (b) DOLU+GAL culture medium

Bacto-yeast nitrogen base without amino acids 6.7 g Glucose 20 gDrop-out mix (x) 2.0 g Distilled water 1000 ml

(x) Drop-out mix: Drop-out mix is a combination of the followingingredients.

Adenine 0.5 g Alanine 2.0 g Arginine 2.0 g Asparagine 2.0 g Asparticacid 2.0 g Cysteine 2.0 g Glutamine 2.0 g Glutamic acid 2.0 g Glycine2.0 g Histidine 2.0 g Inositol 2.0 g Lysine 2.0 g Methionine 2.0 gpara-Aminobenzoic acid 0.2 g Phenylalanine 2.0 g Proline 2.0 g Serine2.0 g Threonine 2.0 g Trytophan 2.0 g Tyrosine 2.0 g Valine 2.0 gIsoleucine 2.0 g

-   (c) DOLU+GLU agar culture medium    -   A solid culture medium prepared by adding 2% (W/V) of agar into        the culture medium-   (a)-   (d) DOLU+GAL agar culture medium    -   A solid culture medium prepared by adding 2% (W/V) of agar into        the culture medium-   (c)    -   “Sequence table free text”    -   SEQ ID No: 9        -   Oligonucleotide primer designed for PCR    -   SEQ ID No: 10        -   Oligonucleotide primer designed for PCR    -   SEQ ID No: 11        -   Oligonucleotide primer designed for PCR    -   SEQ ID No: 12        -   Oligonucleotide primer designed for PCR    -   SEQ ID No: 13        -   Oligonucleotide primer designed for PCR    -   SEQ ID No: 14        -   Oligonucleotide primer designed for PCR    -   SEQ ID No: 15        -   Oligonucleotide primer designed for PCR    -   SEQ ID No: 16        -   Oligonucleotide primer designed for PCR    -   SEQ ID No: 17        -   Oligonucleotide primer designed for PCR    -   SEQ ID No: 18        -   Oligonucleotide primer designed for PCR    -   SEQ ID No: 19        -   Oligonucleotide primer designed for PCR    -   SEQ ID No: 20        -   Oligonucleotide primer designed for PCR    -   SEQ ID No: 21        -   Oligonucleotide primer designed for PCR    -   SEQ ID No: 22 Oligonucleotide primer designed for PCR

1. A cytokinin receptor selected from the group consisting of: (a) acytokinin receptor comprising the amino acid sequence of SEQ ID NO: 6;(b) a cytokinin receptor comprising the amino acid sequence of SEQ IDNO: 2; (c) a cytokinin receptor comprising the amino acid sequence ofSEQ ID NO: 4; (d) a cytokinin receptor comprising the amino acidsequence of amino acids 196 to 1176 of SEQ ID NO: 2; (e) a cytokininreceptor comprising the amino acid sequence of amino acids 50 to 1176 ofSEQ ID NO: 2; (f) a cytokinin receptor comprising the amino acidsequence of amino acids 32 to 1036 of SEQ ID NO: 4; (g) a chimera-typecytokinin receptor comprising extracellular regions, transmembraneregions and histidine kinase regions, all of which are obtained from thesame cytokinin receptor selected from the group consisting of CRE 1,AHK2 and AHK3, and receiver regions which are obtained from thehistidine kinase encoded by the gene selected from the group consistingof S1n1 gene of budding yeast, Chey gene of Salmonella, RcsC gene of E.coli and Phks gene of fission yeast; and (h) a cytokinin receptorcomprising an amino acid sequence that has 95% or higher identity to theamino acid sequence of (a), (b), (c), (d), (e), or (f), wherein saidcytokinin receptor has cytokinin receptor activity.
 2. DNA encoding thecytokin receptor of claim
 1. 3. A transformed cell into which DNA ofclaim 2 has been introduced.